Creado por Cyrielle Saba
hace alrededor de 4 años
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Pregunta | Respuesta |
Nalbuphine K agonist mu antagonist | |
Naloxone antagonist orally inactive | |
naltrexone antagonist orally active | |
Dextromethorphan Mixed agonist/antagonist Lacks analgesia Antitussive activity | |
Meperidine Demerol 25% analgesic activity of morphine | |
Methadone RP=1 Orally active Longer DOA (19 hours) Maintenance therapy + pain suppression of terminally ill patients (cross tolerance) | |
Propoxyphene 10 times less potent than morphine Dextro-->analgesic Levo (-)-->antitussive | |
Loperamide Methadone and Meperidine hybrid Minimal analgesic activity Anti-diarrheal Orally active Very lipophilic but doesn’t enter CNS No central agonist action: Efflux protein P-gp actively Extensive first pass metabolism Low dissolution | |
Propantheline Amino alcohol ester | |
Trihexyphenidyl | |
Phenylephrine a1 agonist | |
Ephedrine a1, a2, b2 agonist | |
Name all mixed opioids | Nalbuphine Pentazocine Cyclazocine Butorphanol Dezocine Dextromethorphan |
Metaraminol a1 agonist | |
Tolazoline a blocker Pheochromocytoma | |
Practolol b1 blocker: effect on isoproterenol tachycardia but not hypotension visual loss | |
Propranolol b blocker 10x more potent than pronethalol | |
Demecarium AChEI | |
Ambenonium AChEI | |
Name all selective B1 blockers | Acebutolol Atenolol Betaxolol Esmolol Metoprolol Bisoprolol NOT METIPRANOLOL |
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